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Items: 1 to 20 of 324

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077274inversion1nstd229human GRCh38 chr11: 10,230,465-10,341,665 , GRCh37.p13 chr11: 10,252,012-10,363,212 ADM, SBF2, 3 more genes
    nsv7073332inversion1nstd229human GRCh38 chr11: 10,230,476-10,341,608 , GRCh37.p13 chr11: 10,252,023-10,363,155 ADM, ADM-DT, 3 more genes
    nsv7072068inversion1nstd229human GRCh38 chr11: 10,355,122-10,355,434 , GRCh37.p13 chr11: 10,376,669-10,376,981 CAND1.11
    nsv7068170inversion1nstd229human GRCh38 chr11: 10,399,499-10,407,669 , GRCh37.p13 chr11: 10,421,046-10,429,216 CAND1.11, RNU6ATAC33P
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv6918081copy number variation1nstd229human GRCh38 chr11: 10,033,455-10,313,724 , GRCh37.p13 chr11: 10,055,002-10,335,271 CAND1.11, ADM, 3 more genes
    nsv6917812copy number variation1nstd229human GRCh38 chr11: 10,345,301-10,372,600 , GRCh37.p13 chr11: 10,366,848-10,394,147 CAND1.11
    nsv6917735copy number variation1nstd229human GRCh38 chr11: 10,398,686-10,398,719 , GRCh37.p13 chr11: 10,420,233-10,420,266 CAND1.11, RNU6ATAC33P
    nsv6917626copy number variation1nstd229human GRCh38 chr11: 10,387,538-10,387,719 , GRCh37.p13 chr11: 10,409,085-10,409,266 CAND1.11
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6916722copy number variation1nstd229human GRCh38 chr11: 10,360,991-10,365,393 , GRCh37.p13 chr11: 10,382,538-10,386,940 CAND1.11
    nsv6914122copy number variation1nstd229human GRCh38 chr11: 10,360,444-10,385,765 , GRCh37.p13 chr11: 10,381,991-10,407,312 CAND1.11
    nsv6908459copy number variation1nstd229human GRCh38 chr11: 10,360,701-10,366,200 , GRCh37.p13 chr11: 10,382,248-10,387,747 CAND1.11
    nsv6906745copy number variation1nstd229human GRCh38 chr11: 10,426,552-10,442,770 , GRCh37.p13 chr11: 10,448,099-10,464,317 CAND1.11
    nsv6904508copy number variation1nstd229human GRCh38 chr11: 10,404,604-10,404,772 , GRCh37.p13 chr11: 10,426,151-10,426,319 CAND1.11
    nsv6902655copy number variation1nstd229human GRCh38 chr11: 10,395,548-10,407,423 , GRCh37.p13 chr11: 10,417,095-10,428,970 RNU6ATAC33P, CAND1.11
    nsv6901043copy number variation1nstd229human GRCh38 chr11: 10,404,667-10,407,283 , GRCh37.p13 chr11: 10,426,214-10,428,830 CAND1.11
    nsv6900402copy number variation1nstd229human GRCh38 chr11: 10,327,475-10,327,665 , GRCh37.p13 chr11: 10,349,022-10,349,212 CAND1.11
    nsv6900084copy number variation1nstd229human GRCh38 chr11: 10,311,136-10,315,879 , GRCh37.p13 chr11: 10,332,683-10,337,426 CAND1.11
    nsv6899425copy number variation1nstd229human GRCh38 chr11: 10,392,601-10,395,500 , GRCh37.p13 chr11: 10,414,148-10,417,047 CAND1.11
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